High molecular composition

ABSTRACT

A HIGH MOLECULAR COMPOSITION COMPRISING A HIGH MOLECULAR SUBSTANCE CONTAINING ONE MEMBER SELECTED FROM THE GROUP CONSISTING OF ALKYL SULFIDE COMPOUNDS AS AN ANTISTATIC AGENT, SAID COMPOUNDS BEING EXPRESSED BY THE FOLLOWING GENERAL FORMULAS A AND B:   (A) R1.S.R2.A(R3-O)NZ   (WHEREIN R1 REPRESENTS A HYDROCARBON RADICAL HAVING 622 CARBON ATOMS; R2 AND R3 EACH REPRESENTS A HYDROCARBON RADICAL HAVING 1-4CARBON ATOMS; A REPRESENTS OXYGEN OR NITROGEN, AND, IN CASE A REPRESENTS NITROGEN, SAID GENERAL FORMULA IS REPRESENTED BY   R1-S-R2-N((-R3-O)N-Z)2   N REPRESENTS AN INTEGER IN THE RANGE OF 0-100; AND Z REPRESENTS HYDROGEN OR COR4 WHEREIN R4 REPRESENTS A HYDROCARBON RADICAL HAVING 1-22 CARBON ATOMS); AND   R1-SO-R2-O-(R2-O)N-H   (WHEREIN R1 REPRESENTS A HYDROCARBON RADICAL HAVING 622 CARBON ATOMS; R2 AND R3 EACH REPRESENTS A HYDROCARBON RADICAL HAVING 1-4 CARBON ATOMS; AND N REPRESENTS AN INTEGER IN THE RANGE OF 0-100).

States Patent Ofice Patented Dec. 5, 1972 3,705,139 HIGH MOLECULAR COMPOSITION Izumi Yamane, Yokohama, Masuzo Nagayama, Tokyo,

and Makoto Takai, Chiba, Japan, assiguors to Lion Fat & Oil Co., Ltd., Tokyo, Japan No Drawing. Filed Oct. 26, 1970, Ser. No. 84,164

Claims priority, application Japan, Oct. 30, 1969, 44/ 86,422, 44/86,423 Int. Cl. C08f 3/02, 7/04, 45/00 US. Cl. 260-923 A 9 Claims ABSTRACT OF THE DISCLOSURE A high molecular composition comprising a high molecular substance containing one member selected from the group consisting of alkyl sulfide compounds as an antistatic agent, said compounds being expressed by the following General Formulas a and b:

R1-g-RrO(R3-O)7LH (wherein R represents a hydrocarbon radical having 6- 22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of -100).

BACKGROUND OF THE INVENTION (a) Field of the invention The present invention relates to an antistatic composition comprising essentially of a high molecular substance, which retains the intrinsic properties of said high molecular substance without any deterioration thereof.

(b) Description of the prior art tlt is generally known that the manufacturing or processing of a high molecular substance or the use of a product comprising essentially of said substance would be accompanied by such electrostatic troubles as dust-catching, electric shock, and so on, 'and as preventive measures therefor, antistatic high-molecular substances are utilized. Said antistatic high-molecular substance is generally prepared by coating, spraying or dipping a solution of some surface active agent having antistatic property on or to a high molecular substance. However, the efficiency of thus produced antistatic high-molecular substance is apt to be temporary and easily deteriorate due to friction, washing, lapse of time, etc. to thereby disappear at last. As a means to sustain the antistatic efliciency, there is known a method of kneading a surface active agent into said substance. Even thus prepared high molecular composition, however, is accompanied by such drawbacks that, the surface active agent runs out in rich amount onto the surface of the composition to make the surface soft and sticky, impede the transparency thereof, deteriorate the intrinsic characteristics of high molecular substance such as strength, thermal resistance, stability against light,

heat and oxidation, and so forth. This is attributable to a functional defect of a conventional surface active agent hitherto employed as an antistatic agent. For example, in case of alkylamine-ethylene oxide adduct or compounds composed thereof which are currently popular on market as antistatic agents for use in blending, they are too poor in thermal resistance or thermal stability to mold with a high molecular substance so that they are available only for a limited purpose in polystyrene and ABS resin which require particularly high temperature for molding. In case of polypropylene, polyethylene, or the like, the antistatic agent would run out unceasingly with the lapse of time, to thereby not only impede the transparency and printability but also accelerate the adhesion of dust due to increase in viscosity of the surface thereof. In case of employment for polyvinyl chloride, too, the conventional antistatic agents are possessed of shortcomings, such that they accelerate pyrolysis thereof, and so on.

SUMMARY OF THE INVENTION The present invention is a result of energetic studies on how to make up for the defects in the prior art, and is intended to provide a composition comprising essentially of a high molecular substance that will not only never impede the intrinsic properties of said high molecular substance but also be capable of preventing deterioration of the efiiciency of the substance against light, heat and oxygen and possessed of enduring antistatic property.

In other words, the present invention is to provide an antistatic high molecular composition comprising essentially of a high molecular substance containing one member selected from the group consisting of alkyl sulfide compounds which are expressed by the following General Formulas a and b:

(wherein R represents a hydrocarbon radical having 6- 22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents oxygen or nitrogen, and, in case A represents nitrogen, said general formula is represented by n represents an integer in the range of 0-100; and Z represents hydrogen or COR, wherein R represents a hydrocarbon radical having 1-22 carbon atoms); and

(wherein R represents a hydrocarbon radical having 6- 22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100).

The composition according to the present invention is prepared by means of kneading a compound represented by the foregoing general formulas into a high molecular substance.

Among al kyl sulfide compounds applicable in the present invention that are expressed by the foregoing General Formula a, a compound wherein A represents oxygen can be prepared by causing a long-chain al kyl mercaptan to react with an al-kylene oxide such as, for instance, ethylene oxide, propylene oxide, or the like in the presence of caustic alkaline catalyst by a conventional method at a temperature in the range of -l30 C. The same can also be prepared by adding an alkylene oxide to a longchain alkyl [s-hydroxyethyl sulfide obtained by combining a hydroxyalkyl mercaptan such as, for instance, [ii-hydroxyethyl mercaptan as a radical with a long-chain aolefin in the same way as above.

A compound wherein Z represents COR, can be prepared by causing a carboxylic acid chloride or acid anhydride to react with the product prepared as above.

A compound wherein A represents nitrogen can be pre pared through the process that: a long-chain alkyl hydroxyalkyl sulfide is prepared by effecting radical reaction between a long-chain olefin and hydroxyalkyl mercaptan by the method mentioned above; subsequently, by adding thionyl chloride to this hydroxyl radical at a low temperature and thereafter heating the admixture to 40 C., a long-chain alkyl chloroalkyl sulfide is produced. By causing this product to react with a dialkanol amine such as, for instance, diethanolamine, and, if necessary, also with alkylene oxide in the presence of caustic alkaline catalyst at 100 C., whereby there is produced a compound to be expressed by the foregoing general formula wherein Z represents hydrogen. A compound prepared through esterification of the foregoing compound by means of a carboxylic acid anhydride or carboxylic acid chloride, such as, for instance, a compound prepared by applying acetic anhydride as an esterifying agent, may also be served for the purpose of the present invention.

Alkyl sulfide compound according to the General Formula b, on the other hand, can be prepared by causing a sulfide according to the General Formula 9. obtained by the aforesaid method to react with a peroxide such as, for instance, hydrogen peroxide. This reaction is effected, at a high rate of yield, by adding hydrogen peroxide to an aqueous solution or an aqueous dispersion of said sulfide at 50 C.

The foregoing process of preparing the compounds according to the present invention can be expressed by the following chemical formulas, but it is not limited thereby.

R-CH=CH2 HSCHsCHzOH L R-CHgCHzSCHgCHzOH ROHQCHQSCHZCHZOH nCH CHg R'CHQCH2S-CH2CH2O(CH CH2OM2H R-CHzOHzSCHzCHsO(CHzCHzOM, H0001 T RCHZCHZ S CH OHzO (CHZCHQOMH In the foregoing general formula, R represents hydrocarbon radical having 6-22 carbon atomspreferably having 10-20 carbon atoms. The compound having carbon atoms less than 6 has an unsatisfactory thermal stability as well as compatibility with a high molecular substance such as plastics, while the other compound having carbon atoms more than 23 is currently hard to obtain as a raw material and cannot be employed profitably from an industrial point of view. As to A representing oxygen or nitrogen, it makes little difference whichever is employed, from a viewpoint of efficiency. As to n representing an integer ranging from to 100, in most cases it is desirable tha said in ger be in the range of 2-50 for moldings such as film, injection-molding product, extrusion-molding product, blow-molding product, etc. and 15-100 for synthetic fibers. However, inasmuch as the integer represented by n is related with R it is advisable that the integer be selected from a fairly wide range, and the integer for synthetic fibers which are generally subjected to frequent washing be bigger than that for molding which are subjected to less frequent washing.

The amount of alkylsulfide to be kneaded into a high molecular substance used in the present invention somewhat varies with the ntaure and shape of a high molecular substance employed, but it is more than about 0.01% of the latter. The optimum amount of said alkyl sulfide to be generally employed for the purpose of antistatic means is in the range of, for instance, 0.01-0.3% for a low-density polyethylene having a density in the range of 0.91-0.93, 0.5-0.7% for a high-density polyethylene having a density in the range of 0.93-0.98, 0.51.0% for polypropylene, 1.53% for polystyrene, acrylonitrilebutadiene-styrene copolymer (ABS resin), polymethacrylate and acrylonitrile-styrene copolymer (AS resin), 1.5-2.5 for rigid polyvinyl chloride, 0.1-0.5% for nonrigid polyvinyl chloride, and 1.2-5 for a synthetic fiber such as nylon, polyester or polyacrylonitrile.

Suitable high molecular substances applicable in the present invention, include well-known resins or rubbers such as, for instance, polyvinyl acetate, polyamino acid, polyamide, polybutadiene and polyisoprene as well as copolymers and mixtures thereof, besides the aforesaid polymers. Furthermore, high molecular compositions according to the present invention may be mixed with pigment, filler and other additives.

Alkylsulfide for use in a high molecular composition comprising a high molecular substance under the present invention is possessed of not only an excellent antistatic property but also a satisfactory compatibility with a high molecular substance, and is so stable at a high temperature that the transparency or the color tone of the high molecular substance will never get impeded. Besides, it has been found that alkylsulfide is capable of preventing deterioration of the intrinsic property of a high molecular substance against heat, oxidation and light, though the mechanism of this effect of alkylsulfide is yet to be clarified. Further, improvement of the Wetting property, abrasiveness and surface polarity of the surface of a high molecular substance and a resultant enhancement of its practical properties such as anti-stain property, anti-fog property, cleansability, adhesiveness, printability, dyeing affinity, flexibility, smoothness, platability for plastic, etc. can be also expected from the employment of said alkylsulfide.

PREFERRED EMBODIMENTS OF THE INVENTION Given hereunder are concrete examples embodying the present invention. In this connection, the measurement of the antistatic property and so on was conducted according to the following procedures.

Measurement of the antistatic property A sample is placed within a 10,000-volt electrostatic field to effect electrification, and is thereafter taken out and measured for its charged voltage and half-value period thereof by continuously observing the state of decaying electricity by means of Static Honestometer (a manufacture of Shishido Shokai Co., Japan). In case the half-value period is less than 4 seconds, it is considered that there occurs no such electrostatic troubles as dust-catching, electric shock and the like.

Measurement of compatibility Under the present circumstances where there is no expedient available for measuring the compatibility of the antistatic agent with a high molecular substance under the examples of the present invention, evaluation is conducted through the procedure that the composition is formed into film, a couple of films thus formed are placed one over the other and left standing under a pressure of 500 g./cm. for hours, the strippability of thus treated static pellets by means of a small-sized extrusion-molding machine. Thus obtained pellets were further formed into a 0.01 mm.-thick film by means of a small-sized infiation apparatus. On the other hand, a film was prepared by employing polyethylene alone in the same manfilms is compared with the result of a blank test and those 5 so closely stuck to each other and hard to strip off is ner as in the foregoing. When the both films were comregarded as poor. In this context, the antistatic agent pared, the charged voltage and half-value period thereof, employed for the present invention as well as in the prior the compatibility with the plastics, the degree of coloring art is in itself possessed of tackiness, and, therefore, even by heating (at 120 C. for '6 hours), and the contact when kneaded into a high molecular substance, it runs 10 angle (with droplet of water resting on a film) were as out gradually onto the surface of said substance rendershown in Table 1, respectively. The composition under ing it tacky. Accordingly, it can be said that the less is the present invention not only displayed an improved the tackiness of the antistatic agent, the better the comantistatic property but also proved to be effective as antipatibility thereof. fog agent due to improved wetting property thereof.

TABLE 1 Static Degree 01 Honestometer coloring after Hallheating Amount Voltage value at120 0. Com- Contact added charge period forfi patiangle Antistatlc agent (percent) (v.) (sec.) hours bility (degrees) Blank test. 40 w 2 90 CflHflS'(CHQCHQOMOD CIIHII 0.1 28 4.8 2 Good- 40 II 0.3 28 4.2 2 .-d0-- 010E218(CH2CHIO)IOOCCIIH3S 0.1 21 a s 2 Good- 52 l 0.3 26 2.4 2 d0 30 CnHniS(CHzCHgOhuoCCuHss 0.1 25 3.1 2 Good- H 0.3 25 2.4 2 do 30 C H S(CHQCHiOMMCC HM 0.1 24 3.1 2 Goodl 0.3 23 2.3 ...do 30 (110E 8(CHaCHrOhonCCnHu 0.1 31 5.8 2 Good- 32 ll 0.3 32 3.3 2 -..do-.- 30

CnHuS (CH1CH20)0H 0.1 28 4.0 2 Good- 40 0.3 20 2.2 2 -..do... 30

C sH 1S(CHgCH20)ioH 0.1 24 2.7 2 Good- 30 0.3 22 1.8 2 ".00-.. 30

CIEH:1S(CH2CH20)5H 0.1 22 1.3 2 Gooda CIQHI1S(CH2CH20)3H 0.1 10 0.2 2 Good- 30 0.3 10 01 2 -..do.. 30

CHgCHzOH 0.1 20 0.5 4 Poor 40 0.3 10 01 6 -do 30 CisHflN GHiCHaOH (for comparative use.)

Measurement of the thermal stability Samples are placed in a gear oven and heated at 120 EXAMPLE 2 9 sppclfied 9 Subsequently the degree of A specified amount of the respective antistatic agent coloring 1s udged with naked eyes and evaluated by L a 1 in a fade criterion whereunder a Sam 16 deve1 listed 111 Table 2 was added to pellets of a high-density 3 y 5 is re arded as fade 1 Whilep the one polyethylene (a manufacture of Showa Denko K.K. mar- ?30 t cons icousl de elo in a color into black is reketed under the brand name Sholex 503W) mixed d as prade 6 p g therewith by means of Henschel mixer for 3 minutes, and ga e g EXAMPLE 1 the mixture was subsequently formed into antistatic pellets by means of a small-sized extrusion-molding ma- A specified amount of the respective antistatic agent chine. Thus obtained pellets were further formed into a listed in Table l was added to pellets of a low-density 2 mm.-thick sheet by means of an injection-molding mapolyethylene (a manufacturer of Mitsubishi Yuka K.K. chine. On the other hand, a film was prepared by emmarketed under the brand name Yukalon K3215), ploying polyethylene alone in the same manner as in mixed therewith by means of Henschel mixer for 3 minthe foregoing. The result of evaluation conducted in the utes, and the mixture was subsequently formed into antisame way as in Example 1 was shown in Table 2.

TABLE 2 Degree of Static Honestometer coloring after Halfheating Amount Voltage value at 120 0. Comadded charged period for 6 pati- Antlstatlc agent (percent) (v.) (see.) hours bility Blank test 40 w 2 C15H;1S(CH:CH20)10H O. 33 4. 3 Good.

CH; 0. 5 23 2. 8 1 Good. I 0. 7 18 1. 2 1 D0. C1rH 1S(OH:CHzO):CHzCHOH C1:H37S(CH:CH;O) H 0. 5 16 0 8 1 Good.

CHZCHQOH 0.5 18 0 9 5 Poor. 0. 7 12 0 5 5 D0. Cu a1 CH ClLOH (for comparative use).

EXAMPLE 3 Evaluation Was conducted with respect to polypropylene (a manufacture of Mitsubishi Yuka K.K. marketed under the brand name Mitsubishi Noblene MA-4) in the same Way as in Example 2, and the result was as shown in Table 3.

TABLE 3 Degree of Static Honestometer coloring after Halfheating Amount Voltage value at 120 0. Comadded charged period for 6 pati- Antistatic agent (percent) (v. (sec.) hours bility Blank test 40 w 2 OH CH OH 0. 6 38 '1. 3 2 Good 1.0 36 2. 3 2 Do. CIZHHS CHzCHzN CHiCHgOH (CH CHgOhH 0. 5 32 3. 6 2 Good.

1. 0 1. 7 2 Do. C12 z5S CHrC 2N (CHaCHzOhH (113E378 (CHzCHzO)zH 0. 5 30 2. 8 1 Good.

CEZCHZOH 0. 5 4. 8 5 P001. 1. 0 32 1. 0 5 Do. Cns u CHQCHZOH (for comparative use).

Evaluation was conducted with respect to polystyrene (a manufacture of Mitsubishi-Monsanto Kasei K.K. marketed under the brand name Diarex HF-77), ABS resin (a manufacture of Mitsubishi-Monsanto Kasei K.K. marketed under the brand name Lustran), methyl meth- EXAMPLE 4 acrylate resin (a manufacture of Sumitomo Kagaku K.K.

TABLE 4 Amount St atle Honestometer Degree of of anticoloring static Halialter agent Voltage value heating Transadded charged period at 120 C pareney Resin Antistatie agent (percent) (sec for 6 hours (percent) Polystyrene Blank test 40 w 2 0101121 S (CHaGHzOhH 2. 0 35 4. 8 1 100 3. O 22 O. 8 1 100 01H S (CBQCH OMH 2. 0 36 4. 0 2 100 3.0 30 0. 8 2 100 CHzCHnOH 2.0 32 5. 6 5 98 a. 0 32 1. 2 6 98 u m CH2CH2OH (for comparative use).

Compatibility Degree of coloring Haltafter value heating period at 120 C. (see) tot 6 hours TABLE 4Continued Amount Static Honestometer oi antistatic agent Voltage added charged Antistatic agent (percent) (v.)

Acrylonitrile-butadiene-styrene copoly- Blank test.

010E215 (CHzCHqOMH mer (ABS resin).

Resin CHQCHIOH CiaHn resin).

Acrylonitrile styrene copolymer (ABS C is s'l CHZCHROH (for comparative use).

Pol eth lmethacrylate (MMA resin). Blank test i..

ym y (110E118 (CHzCHzOhH 2.0

CmHesS (CHnCHaOhH CH2CH2OH fiiciency Degree of coloring alter Haltheating value at 120 0. period for 6 (sec) hours Thus obtained pellets were further formed into IS-denier filaments by means of a small-sized melt spinning machine. On the other hand, filaments were prepared employing nylon alone in the same manner as in the foregoing. The result of evaluation of the antistatic e and thermal stability (degree of coloring) of the both filaments was as shown in Table 5.

TABLE 6 Static Honestometer Amount Voltage added charged (percent) (v.)

meni'omfi """"""'iis' as 3.0 23

listed with b by means of a small-sized extrusion-molding machine. 40

50 Law CroHnS (CH2C 2 )a 00 Law C 11 S (CHzCHaOMuoC C11Hz5 C Hn S (CHnCH2O)1ouC 011 35 (for comparative use).

1 1 EXAMPLE 6 Evaluation was conducted with respect to polyester in the same way as in Example 5, and the result was as shown in Table 6.

keted under the brand name Vinika), 20 parts by weight of dioctyl phthalate (DOP), 1.5 parts by weight of Ba stearate and 0.5 part by weight of Cd stearate, and the mixture was kneaded with a small-sized roll-knead- TABLE 6 Degree of Static Honestometer coloring after Halfheating Amount Voltage value at 120 0. added charged period for 6 Antistatie agent (percent) (sec) hours Blank test. 40 w 2 02011 S (CHzCHzOhaufi 011B 3. 22 1. 8 2

CuHnS (CH:CHzO)5u(|J 017B 3. 0 l. 0 2

EXAMPLE 7 20 ing machine for 5 minutes and formed into a 1 mm.-

A fixed amount of the respective antistatic agent listed in Table 7 was added to a solution prepared by dissolving 10 parts by weight of acrylonitrile-vinyl chloride c0- polymer in 100 parts by weight of acetone and thoroughly dissolved therein. The resultant solution was spread on a glass plate and dried with a hot blast, thereby forming a film. The result of evaluation of the antistatic efiiciency of thus prepared film was as shown in Table 7.

thick sheet of rigid polyvinyl chloride respectively by means of press-molding. A specified amount of the respective antistatic agent listed in Table 8 was added to a composition comprising 100 parts by weight of polyvinyl chloride powder (a manufacture of Mitsubishi-Monsanto Kasei K.K. marketed under the trade name Vinika), parts by weight of DOP, 1.5 parts by weight of Ba stearate and 0.5 part by weight of Cd stearate, and the mixture was kneaded with a small-sized bench roll-knead- TABLE 7 Degree of Static Honestometer coloring after Haiiheating Amount Voltage value at 120 0 added charged period (or 6 Antistatic agent (percent) (vi) (sec.) hours Blank test. 40 w 2 CnHn S (CH2CH2O)XOB(HJC11HZE 3. 0 28 2. 0 2

01: :78 2 2 M CnHar 3. 0 24 1. 1 2

EXAMPLE 8 ing machine for 5 minutes and formed into a 1 mm.-thick A specified amount of the respective antistatic agent listed in Table 8 was added to a composition comprising parts by weight of polyvinyl chloride powder (a manufacture of Mitsubishi-Monsanto Kasei K.K. marsheet of non-rigid polyvinyl chloride, respectively, by means of press-molding. These sheets were heated at C. for 2 hours, and the degree of their coloring was surveyed. The result was as shown in Table 8.

TABLE 8 Static Amount Honcstometer Degree of of anticoloring static Halfalter agent Voltage value heating Comadded charged period at 120 C. pati- Resin Antistatic agent (percent) (v.) (see) for 2 hours bility Blank test 40 m 4 CuHuS-CHgCH3OCHgC|HOH 2.0 28 1.1 3 GOOd Rigid PVC C H S (CHgCHgO)lCH3C|HOH 2. 0 24 1. 8 3 Good.

CuHz5S(CHgCHgO)3H 2.0 22 0.7 3 Good.

CguHnS (CHzCHgO)mCC17H35 2. 0 18 1.8 3 (300d.

C13Ha7S(CHzCH O)aH 2. 0 12 0. 1 3 Good.

CHzCHgOH 2.0 18 1. 0 5 Poor.

CHQCHZOH TABLE 8Continued Amount Honestometer Degree oi of anticoloring static Haliafter agent Voltage value heating Comadded charged period at 120 C. pati- Resin Antistatic agent (percent) (v.) (sec.) for 2 hours bility Nonrigld PVC Blank test 40 m 4 C Hg5S-CH,CH,OCH,([JHOH 1.0 22 1.0 3 Good.

CnHaaS (CHzCHgOhCHflfHOH 1.0 23 0.9 3 GOOd.

011E 5 (OHgCH20);H 1.0 21 0.8 3 Good.

020E418 (CHgCH O) C CuHu 1. 0 1. l 3 Good.

C 5H31S(CHgCHzO) H l. 0 12 0. l 3 GOOd- CHgCHgOH 1. 0 21 0.9 5 Poor.

Cm n

0 H O HzQH (for comparative use).

EXAMPLE 9 EXAMPLE 10 The antistatic plastics prepared by kneading as in Examples 1, 2 and 3 were subjected to tension test by means of Tensilon universal tension tester (a manufacture of Toyo Sokki K.K.). Further, they were subjected to ultraviolet-ray radiation for 20 hours and 50 hours by means of Weather-O-Meter (a manufacture of Toyo Seiki K.K.), and their elongation and tensile strength were measured thereafter. The results are shown in Table 9 in terms of the numerical value obtained by dividing post-radiation property of matter by pre-radiation property of matter and multiplying the quotient by 100, that is, the preservation ratio of the property of matter. As seen from this table, the property of these compositions are remarkably prevented from getting deteriorated by virtue of kneading therein the compounds according to the present invention.

TABLE 9 The same nylon filament as in Example 5 was wound on a spool repeatedly and the coil of nylon filament was cut off both ends to be a bundle 10* cm. by 5 cm. in dimension. The resultant bundle of nylon filament, upon fixing the both ends thereof by means of a bonding agent lest it should get loosened, was served as a test piece. (This test piece Weighed 2.5 gr.)

The foregoing test piece was settled on a retainer while sustained in the form of strain at the both ends thereof, and dipped in a polluting bath below-mentioned at a temperature of 20-25 C. for 24 hours. Subsequently, thus treated filament coil was taken out from said bath and air-dried, and thereafter, the refractive index thereof was determined by means of a photodilfraction meter. The polluting bath becomes free from foaming by means Preservation ratio of property of- Amount of Matter after hours Matter after 200 hours antistatig radiation (percent) radiation (percent) agen added Elon- Tensile Elon- Tensile Resin Antistatic agent percent tion strength gation strength Low-density polyethyl- Blank test 47. 5 53. 8 22. 0 28. 8 ans. CmHuS CH2CH20 5H 0. 3 140. 0 120. 6 85. 0 90. 4 C HnSwHrCHzOhH 0. 3 153. 0 125.6 90. 6 96. 3 C HwNwHzCHzOHh 0.3 56. 2 54. 6 27. 6 29. 6

High-density polyethyl' Blank test 52. 3 58. 7 25.3 29. 1 ene. C 5H 1S(CH1CH20)1H 0. 7 136. 4 129. 3 96. 3 91. 8 ounnmonrontonh 0.7 51. 1 54. 4 25. 4 26. 3

Polypropylene Blank test 38. 4 34. 6 C18H37S CH2CH20 9H 1. 0 120. 1 118. 6 C gHz1N(CHzCHzOH)2 1. 0 31. 6 35. 4

of washing mens soiled underwears (5 pieces of cotton goods) and Working clothes (cotton goods; a couple of suits of coat and trousers) with an electric washing machine by using 0.2% aqueous solution of an anionic prepared by employing polyethylene alone in the same manner as in the foregoing. Subsequently, the voltage charged as well as half-value period thereof, the compatibility, the degree of coloring by heating (at 120 C. for

detergent at C. and thoroughly stirring for 20 min- 5 6 hours), and so on were judged for the both films. The utes. The result was as shown in Table 10. As seen from result was as shown in Table 11. As seen from this table, this table, the compositions according to the present inventhe compositions according to the present invention not tion are remarkably prevented from pollution. In this only demonstrated an improved antistatic property but connection, the soil additional density (SAD) is equal to also proved effective as antifog agents due to improved 10 wetting property thereof.

TABLE 11 Static Degree of Honestometer coloring after Haliheating Amount Voltage value at 120 0. Com- Contact added charged period for6 patiangle Antistatic agent (percent) (v.) (sec.) hours bility (degrees) Blank test 40 w 2 90 0 0.1 3.8 2 Good 53 T 0.3 28 2.1 2 .do-- 30 Cn u z n )5o 0 0.1 26 2.5 2 Good 40 T 0.3 24 1.3 2 -do.. 30 01311315 2 2 10H 0 0.1 24 1.0 2 Good T 0.3 22 0.2 2 do 30 013 31 5 2 z )s 0 0.1 12 0.2 2 Good 30 T 0.3 12 0.1 2 mac... 30 011 S (CH2CH:O)3H

omcmoH 0.1 20 0.5 4 Poor... 0.3 1.0 01 3 ..do 30 C1s a7 CHZCHgOH (for comparative use).

EXAMPLE 12 ic B5 A specified amount of the respective antistatic agent (wherein R represents the initial index of refraction and listed in Table 12 was added to pellets of a high-density R represents the postapollution index of fraction). polyethylene (a manufacture of Showa Denko K.K. mar- TABLE 10 Index of refraction Soil additional Amount Post density added pollu- AD Antistatie agent (percent) Initial tion X10 nk test 86.4 72.9 738 1a z1 sCHzO)moH 3.0 85.1 79.9 276 (32911413 (CHgCHgO) 100% 0171135 3. O 86. 3 81. 6 241 EXAMPLE 11 l eted under the brand name Shorex 30), mixed therewith by means of Henschel mixer for 3 minutes, and A sPeclfied amount of the respectlve antlstatlc agejnt the respective mixture was subsequently formed into antihsted in Table 11 was added to pellets of a lcyw'denslty static pellets by means of a small-sized extrusion-molding polyethylem (a manufactuge of i 5 machine. Thus obtained pellets were further formed into marketed under the bran name u a on a 2 mm.-thick sheet, respectively, by means of an mixed therewith by means of Henschel mixer for 3 minutes, and the respective mixture was subsequently formed into antistatic pellets by means of a smallsized extrusionmolding machine. 'I h-us obtained pellets were further formed into a 0.01 mm.-thick film, respectively, by means injection-molding machine. Another film was prepared by employing polyethylene alone in the same manner as in the foregoing. The result of evaluation conducted for the both films in the same Way as in Example 11 was as of a small-sized inflation apparatus. Another film was shown in Table 12.

TABLE 12 Degree of Static Honestometer coloring after Halfheating Amount Voltage value at 120 C. Cornadded charged period for 6 pati- Antistatic agent (percent) tv.) (see) hours bility Blank test 40 w 2 O 32 3.2 2 Good. T 0 7 1.1 2 Do. CIBHN S 2 C 2 D10 O CE; 0.5 24 2.6 2 Good. g 1 0. 7 19 1. 0 2 D0. C1aH 7 (CHgCHgOh-CHgCHO O 0. 5 18 0. 8 2 Good." T 0 7 12 0. 5 2 Do. 0 5E3 8 (CH CH OhH CHgCHgOH 0. 5 18 0.9 5 Poor. 0.7 12 0. 5 5 Do. Crs a1N CHQCHZOH (for comparative use).

EXAMPLE 13 manufacture of Mitsubishi-Monsanto Kasei K.K. marketed Evaluation was conducted with respect to polypropyl 5 under the brand name Lustran,,) methyl methaorylate igf g gggg gg z g g i i mg j fi fig resin (a manufacture of Sumitomo Kagaku K.K. marketed the same way as in Example 12, and the result was as under the brand name Sumlpex L0,) and acrylonitrile shown in Table 13.

TABLE 13 Static Honestometer Degree of coloring Haliafter heat- Amount Voltage value ing at employed charged period 120 C. for Compati- Antistatic agent (percent) (v.) (sec.) 6 hrs. bility Blank test 40 w 2 O 0.5 3.3 1 Good. T 1.0 28 0.2 1 Do. 015 318 2 2 )aH CHgCHgOH 0 5 32 5.6 5 Poor. 1 0 32 1.2 6 Do. CiaHa1N CHgCHzOH (for comparative use).

EXAMPLE 14 45 styrene copolymer resin (a manufacture of Daiseru K.K. Evaluation was conducted with respect to polystyrene marketed under the brand name Sebian-N) in the same (a manufacture of Mitsubishi-Monsanto Kasei K.K. marway as in Example 12, and the result was as shown in keted under the brand name Diarex HF"), ABS resin (at Table 14.

TABLE 14 Amount Static Honestometer Degree of of anticoloring static Halfafter agent Voltage Value heating Transadded charged period at 120 C. parency Resin Antistatie agent (percent) (v.) (sec.) for 6 hrs. (percent) Polystyrene Blank test 40 m 2 100 O 2. 0 4. 4 2 100 T 3. 0 26 1. 0 2 100 C10H2rS(CH2CH2O) H O 2. 0 34 3. 8 2 100 T 3. O 28 0. 9 2 100 CtHlsS (CHzCHzWa CHzCHsOH 2. 0 32 5 6 5 98 3. 0 32 1 2 6 98 C1s a7 CH2CII3OH (for comparative use).

ABS resin Blank test w 0 2. 0 84 2. 8 T 3. 0 0. 6 C1oHn1S(CH2CHaO) H CHzCHzOH 2.0 35 4.0 3. 0 30 1. 0 CmHayN CHzCHaOH (for comparative use).

TABLE 14Continuerl Amount Static Honestometer Degree of of anticoloring static I-Ialfafter agent Voltage value heating Transadded charged period at 120 C. parency Resin Antlstatic agent (percent) (v.) (sec.) for 6 hrs. (percent) AS resln Blank test 40 w 2 100 2.0 34 4.5 2 99 T 3.0 23 0.9 2 09 0101121 S (CHzOHzOhH 0 2.0 35 4.2 2 99 T 3.0 28 0.7 2 98 010 03 2C z )aH CHzOHzOI-I 2. 0 36 5.0 5 95 3.0 31 1.3 6 93 CisHnN onzonzon (for comparative use).

MMA resln Blank test 40 w 2 100 0 2.0 34 4.7 2 100 T 3.0 26 0.9 2 100 CaHi1 )s 0 2.0 38 4.2 2 100 T 3.0 29 0.8 2 100 CnHayS (CHaCH)sH CHzCHzOH 2.0 36 5.4 5 95 3.0 31 2.1 6 05 CuHavN CHQCHQOH (for comparative use).

EXAMPLE 15 TABLE 16 A specified amount of the respective antistatic agent 35 Static listed in Table 15 was added to nylon pellets, mixed Honestometer therewith by means of Henschel mixer for 3 minutes, and H lf. the respective mixture was subsequently formed into anti- Amount Voltage Value Degree added charged period of stat1c pellets by means of a small-sized extrusion-molding 4O Anti t ti agent (percent) (v (Sm) coloring 1 machine. Thus obtained pellets were further formed into Blank test m 2 a 15-denier filament respectively by means of a smallsized melt spinning machine. The result of evaluation of 26 2 the antistatic efiiciency and thermal stability (degree of O15H31S(CHlOH20)100H colorlng) of these filaments was as shown 1n Table 15. T 30 25 L3 2 TABLE 15 CIBHB1S(CH2CH20)50H st ti 1 After heating at 120 C. for 6 hours. Honestometer EXAMPLE 17 Half- Amggng 01m valug Degree A specified amount of the respective antistatic agent a e 0 3X28 perlo 0 Anflstatic agent (percent) (V (Sec) 6010 ri ngl listed in Table 17 was added to a solution prepared by dis solving 10 parts by weight of acrylomtnle-vmyl chloride Blank test 40 2 copolymer in 100 parts by weight of acetone and (T) 1.8 32 g g thoroughly dissolved therein. The resultant solution was OMHMS (CHCHZOMODH spread on a glass plate and dr1ed with a hot blast, thereby forming a film. The result of evaluation of the ant1stat1c 1:8 3; g efiiciency of thus prepared film was as shown in Table 17. OnHa1S(CH2CH20)so TABLE 17 0 1.5 34 4.6 2 static T 3.0 28 1.4 2 010E517 S (CHzCHg 00H Honestometer Half- O 3 Amount Voltage value Degree H T CH OH O H added charged period of 01s s1 I I )3 Antistatic agent (percent) (v.) (sec.) coloring 0H CH 0 H 1.5 40 71.4 4 1 a )w 3.0 36 8 6 Blank test 40 m 2 01813811 3. o 20 2. 1 2

(CHOH:O)5H (110 31 S (CH2CH20)io0 (for comparative use). 0 3' 0 25 1 2 2 1 After heating at 120 C. for 6 hours. CISHwg (0 H30 H10) 50H EXAMPLE 16 1 After heating at 120 C. for 6 hours.

Evaluation was conducted with respect to polyester in the same way as in Example 15; The result was as shown in Table 16.

EXAMPLE 18 A specified amount of the respective antistatic agent listed in Table 18 was added to a composition compris- 21 ing 100 parts by weight of polyvinyl chloride (a manufacture of Mitsubishi-Monsanto Kasei K.K. marketed under the brand name Vinika), 20 parts by weight of DOP, 1.5 parts by weight of Ba stearate and 0.5 part by weight 22 spectively, by means of press-molding. Subsequently, these sheets were heated at 120 C. for 2 hours, and the degree of their coloring was surveyed. The result was as shown in Table 18.

TABLE 18 Hon siaiii ieter Degree of coloring Amount Voltage i l: heftiii added charged period at 120 C. Oompa t- Resin Antistatic agent (percent) (v (sec.) for 2 hrs. ibility Rigid PVC Blank test- 40 w 4 CH1 2. O 26 1.3 3 Good. C1211; CHgCH O CHfl JHOH O CH; 2. 0 22 1. 6 3 D0 CuHzs (CH2CHIO)3CH1$HOH O 2. 0 0. 1 3 D0. 12 (OH2CH2O)3H O 2. 0 14 0. 1 3 D0. 015E137 ST (CHRCHZO) 3H CHqCHgOH 2.0 18 1.0 5 Poor.

C1s a7N CHgCHzOH (for comparative use).

Nonrigid PVC Blank test. 25.0 4

0 CH: 1.0 18 1.0 3 Good. CnHn CHgCHQO CHA JHOH 0 CH3 1. 0 16 0. 8 3 D0. 01 E 12 (CHzCHgOhCHgHOH O 1. 0 18 1. 1 3 Do. 12Has (CHgCH O)3H O 1. 0 17 0. 8 3 Do. C aHa7 (CHgCH2O)zH CH CH OH 1.0 20 1.0 5 Poor.

CrxHtlN CHzCHzO H (for comparative use).

of Cd stearate, and the mixture was kneaded with a small- EXAMPLE 19 sized roll-kneading machine for 5 minutes and formed into a 1 mm.-thick sheet of rigid polyvinyl chloride, respectively, by means of press-molding. Another specified amount of the respective antistatic agent listed in Table 18 was added to a composition comprising 100 parts by weight of polyvinyl chloride powder (a manufacture of Mitsubishi-Monsanto Kasei K.K. marketed under the brand name Vinika), parts by weight of DOP, 1.5 parts by weight of Ba stearate and 0.5 part by weight of Cd stearate, and the mixture was kneaded with a small sized roll-kneading machine for 5 minutes and formed into The antistatic plastics prepared by kneading as in EX- amples 1, 2 and 3 were subjected to tests for elongation and tensile strength subsequent to ultraviolet-ray radiation for 20 hours and 50 hours by means of Tensilon universal tension tester (a manufacture of Toyo Seiki K.K.). The results are shown in Table 19 in terms of the preservation ratio (viz numerical value obtained by dividing post-radiation property of matter by pre-radiation property of matter and multiplying the quotient by 100). As seen from this table, the compositions according to the present invention are remarkably effective in preventing the deteria 1 mm.-thick sheet of non-rigid polyvinyl chloride, reoration of polyethylene and polypropylene.

TABLE 19 Preservation ratio of Preservation ratio of Amount property of matter property of matter of antiafter hrs. radlaafter 200 hrs.

static tion (percent) radiation agent added Elonga- Tensile Elonga- Tensile Resin Antlstatlc agent (percent) tion strength tion strength Low density polyethylene Blank test 47. 5 53. 8 22.0 28. 8

(T) 0. 3 130. 4; 111. 1 80. 3 88. 2 C1aHa7 S (CH2CH2O) H (T) 0. 3 144. 6 115. 4 85. 7 92. 3 C1aH31S(CHaCHzO)3H C1aH; N(CH,CH,OH)z 0. 3 56. 2 54. 6 27. 6 29. 6

TABLE l9-Continued Preservation ratio of Preservation ratio of Amount property of matter property of matter of antiafter 100 hrs. radiaafter 200 hrs.

statit tion (percent) radiation agen added Elonga- Tensile Elonga: Tensile Resin Antistatic agent (percent) tion strength tion strength High density polyethylene Blank test 52. 3 58. 7 25. 3 29. 1

(T) 0. 7 126. 4 119. 7 91. 4 87. 3 ClBHa'l S (CH2CH:O) H

C15H37N CHZCH2OH)2 0.7 51.1 54. 4 25. 4 26. 3

Polypropylene Blank test 38. 4 34.6

(T) 1. 110. 6 110. ClBHal S (CI-IzCHzOhH Cl3H37N(CH2OHzOH)2 1.0 31.6 35.4

EXAMPLE 20 20 group consisting of compounds being expressed by the The same nylon filament as in Example was wound on a spool repeatedly and the coil of nylon filament was cut off both ends to be a bundle 10 cm. by 5 cm. in dimension. The resultant bundle of nylon filament, upon fixing the both ends thereof by means of a bonding agent lest it should get loosened, was served as a test piece. (This test piece weighed 2.5 gr.)

The foregoing test piece was settled on a retainer while sustained in the form of strain at the both ends thereof, and dipped in a polluting bath below-mentioned at a temperature of -25 C. for 24 hours. Subsequently, thus treated filament coil was taken out from said bath and air-dried, and thereafter, the refractive index thereof was determined by means of a photodiffraction meter. The polluting bath becomes free from foaming by means of washing therein mens soiled underwears (5 pieces of cotton goods) and working clothes (cotton goods; a couple of suits of coat and trousers) with an electric washing machine by using 0.2% aqueous solution of an anionic detergent at 25 C. and thoroughly stirring for 20 minutes. The result was as shown in Table 20. As seen from this table, the compositions according to the present invention are remarkably prevented from pollution. In this connection, the soil additional density (SAD) is equal to log (wherein R represents the initial index of refraction and R represents the post-pollution index of refraction).

What we claim is:

1. A composition consisting essentially of a high molecular weight synthetic moldable thermoplastic polymer and as an anti-static agent, one member selected from the following General Formulas a and b:

( R -S-R -A-(R O)nZ (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents one member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said general formula is represented by (Ra-O) RyS'RZN (R$O)1LZ n represents an integer in the range of 0-100; and Z represents one member selected from the group consisting of hydrogen and COR wherein R represents a hydrocarbon radical having 1-22 carbon atoms); and

0 (b) R,-sR2-o(R3-0)nH (wherein R represents a hydrocarbon radical having 15-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100) 2. A composition according to claim 1, wherein the amount of said member is more than about 0.01% by weight.

3. A high molecular composition consisting essentially of polyethylene having a density in the range of 0.91- 0.93, said polyethylene containing as an anti-static agent OBI-0.3% Weight of one member selected from the group consisting of compounds expressed by the following General Formulas a and b:

(a) R -S -A-(R O)nZ (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents one member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said general formula is represented by (Ra-(D772 RXS'RZN (R3O)7LZ n represents an integer in the range of 0-100; and Z represents one member selected from the group consistmg of hydrogen and COR wherein R represents hydrocarbon radical having 1-22 carbon atoms); and O (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100) 25 4. A high molecular composition consisting essentially of polyethylene having a density in the range of 0.93- 0.98, said polyethylene containing as anti-static agent 0.5- 0.7% by weight of one member selected from the group consisting of compounds expressed by the following General Formulas a and b: (a) R -S-R -A-(R O)nZ (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents one member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said general formula is represented by Rs)nZ R -S-Rz-N (Ra-O)nZ n represents an integer in the range of 0-100, and Z represents one member selected from the group consisting of hydrogen and COR wherein R represents a hydrocarbon radical having 1-22 carbon atoms); and

R1 S-R2- 0 (R3O)'TLH (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100) 5. A high molecular composition consisting essentially of polypropylene containing as an anti-static agent 0.5- 1.0% by weight of one member selected from the group consisting of compounds expressed by the following General Formulas a and b:

(wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents one member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said general formula is represented by n represents an integer in the range of O-lOO; and Z represents one member selected from the group consisting of hydrogen and COR wherein R represents a hydrocarbon radical having 1-22 carbon atoms); and

(wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100).

6. A high molecular composition consisting essentially of one member selected from the group consisting of polystyrene, acrylonitrile-butadiene-styrene copolymer, polymethylmethacrylate and acrylonitrile-styrene copolymer and containing as an anti-static agent 1.5-3% by weight of one member selected from the group consisting of compounds expressed by the following General Formulas a and b:

(wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents one member selected from the group consisting of oxygen 7. A high molecular composition consisting essentially of rigid polyvinyl chloride containing as an antistatic agent 15-25% by weight of one member selected from the group consisting of compounds expressed by the following General Formulas a and b:

(a) R -S-R -A-(R O)nZ (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; A represents one member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said general formula is represented by (Rs-0)!LZ RpS-Rz-N (Rs-QUIZ n represents an integer in the range of 0-1'00; and Z represents one member selected from the group consisting of hydrogen and COR wherein R represents a hydrocarbon radical having 1-22 carbon atoms); and

R -SR2-O(Ra-O)1ZH (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100).

8. A high molecular composition consisting essentially of non-rigid polyvinyl chloride containing as an anti-static agent 01-05% by weight of one member selected from the group consisting of compounds expressed by the following General Formulas a and b:

(wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having l-4 carbon atoms; A represents one member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said general formula is represented by (nr-omz R1-S-R2-N (Ra-OMZ n represents an integer in the range of 0-100; and Z represents one member selected from the group consisting of hydrogen and COR wherein R represents a hydrocarbon radical having 1-22 carbon atoms); and

R1-SRz-0(Rl0)7lH (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocarbon radical having 1-4 carbon atoms; and n represents an integer in the range of 0-100) 9. A high molecular composition consisting essentially hydrocarbon radical having l-22 carbon atoms); and of a synthetic fiber forming high molecular weight mod- (b) 0 able thermoplastic polymer and containing an anti-static T agent 1.2-5% by weight of one member selected from R"S R2'O(R3 O)"H the group consisting of compounds expressed by the f l- 5 (wherein R represents a hydrocarbon radical having 6-22 lowing General Formulas a and carbon atoms; R; and R each represents a hydrocar- 1 2 3 bon radical having 14 carbon atoms, and n represents an integer in the range of 0-100) (wherein R represents a hydrocarbon radical having 6-22 carbon atoms; R and R each represents a hydrocar- 10 f r n s C t d bon radical having 1-4 carbon atoms; A represents one UNITED STATES PATENTS member selected from the group consisting of oxygen and nitrogen, and, in case A represents nitrogen, said 2727004 12/1955 Cohen 260 DIG' 019 gemral fmmula 1S Presented by JAMES A. SEIDLECK, Primary Examiner (lb-DMZ 10 J. A. DONAHUE, JR., Assistant Examiner RrS-Ra-N o z U.S. Cl. X.R.

n represents an integer in the range of 0-100; and Z 26075 T, 78 S, 80.7, 85.5 HC, 88.7, 89.5 S, 93.5 A, represents one member selected from the group consist- 20 93.7, 94.7 S, 94.9 G, 584, 607, DIG. 15, DIG. 19 ing of hydrogen and COR wherein R represents a Patent No. 3 79 139 Dated December 5 972 Inventor(s) Izumi Yamane, Masuzo Nagayama and Makoto Takai It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

Column 24, line 50; after "0.3%" insert --by Column 24, line 54; change the formula to read R S-R -A- (R 112 Column 27, line 3; after "containing" insert --as---.

(SEAL) Attest:

ROBERT GOTTSCHALK EDWARD M.FLETCHER,JR.

Commissioner of Patents Attesting Officer FORM USCOMM-DC scam-Pee U.$. GOVERNMENT PRINTING OFFICE; [959 0-355-334 

